Nature Communications (Sep 2023)

Pre-clinical validation of a pan-cancer CAR-T cell immunotherapy targeting nfP2X7

  • Veronika Bandara,
  • Jade Foeng,
  • Batjargal Gundsambuu,
  • Todd S. Norton,
  • Silvana Napoli,
  • Dylan J. McPeake,
  • Timona S. Tyllis,
  • Elaheh Rohani-Rad,
  • Caitlin Abbott,
  • Stuart J. Mills,
  • Lih Y. Tan,
  • Emma J. Thompson,
  • Vasiliki M. Willet,
  • Victoria J. Nikitaras,
  • Jieren Zheng,
  • Iain Comerford,
  • Adam Johnson,
  • Justin Coombs,
  • Martin K. Oehler,
  • Carmela Ricciardelli,
  • Allison J. Cowin,
  • Claudine S. Bonder,
  • Michael Jensen,
  • Timothy J. Sadlon,
  • Shaun R. McColl,
  • Simon C. Barry

DOI
https://doi.org/10.1038/s41467-023-41338-y
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 17

Abstract

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Abstract Chimeric antigen receptor (CAR)-T cell immunotherapy is a novel treatment that genetically modifies the patients’ own T cells to target and kill malignant cells. However, identification of tumour-specific antigens expressed on multiple solid cancer types, remains a major challenge. P2X purinoceptor 7 (P2X7) is a cell surface expressed ATP gated cation channel, and a dysfunctional version of P2X7, named nfP2X7, has been identified on cancer cells from multiple tissues, while being undetectable on healthy cells. We present a prototype -human CAR-T construct targeting nfP2X7 showing potential antigen-specific cytotoxicity against twelve solid cancer types (breast, prostate, lung, colorectal, brain and skin). In xenograft mouse models of breast and prostate cancer, CAR-T cells targeting nfP2X7 exhibit robust anti-tumour efficacy. These data indicate that nfP2X7 is a suitable immunotherapy target because of its broad expression on human tumours. CAR-T cells targeting nfP2X7 have potential as a wide-spectrum cancer immunotherapy for solid tumours in humans.